A NANOFIBROUS HYDROGEL FOR BONE TISSUE ENGINEERING Umadevi Kandalam, PhD Assistant Professor Department of Pediatric Dentistry College of Dental Medicine Nova Southeastern University Fort Lauderdale, Florida
Various Craniofacial Defects Cleft Defect- Hard Palate Alveolar Cleft Alveolar Cleft Craniosynostosis
Tissue Engineering CELLS SCAFFOLD Signals
Growth factors Mammalian cells Tissue Engineering Three dimensional scaffold Micron/nano size and interconnected pores Osteoconductive Mechanically strong Biocompatible and biodegradable Bone regeneration In vitro culture of cells on scaffold
GOAL REPAIR THE BONY DEFECT IN THE CRNIOFACIAL REGION USING TISSUE ENGINEERING TECHNIQUES
STEM CELL Stem Cell Self renew Progenitor Cell Terminally differentiated Cell
EMBRYONIC STEM CELLS
ADULT STEM CELLS
MESENCHYMAL STEM CELLS
MESENCHYMAL STEM CELLS MSCs potential alternatives to the conventional methods Dexamethasone Indomethacin Insulin IBMX CD44, CD73, CD90 and CD105 +ve Dexamethasone High Glucose, TGF-β, ITS Insulin FGF Dexamethasone Ascorbic acid Β- Glycerophosphate
MESENCHYMAL STEM CELLS FROM OROFACIAL REGION Bone marrow is traditional stem cell source for bone tissue engineering Enzymatic Digestion-Isolation of cells Human Gingiva Recently, human gingival mesenchymal stem cells (HGMSCs) have been shown to be superior HGMSCs Neural crest derived High Proliferation Osteogenic differentiation Immunomodulation
Tissue Engineering CELLS SCAFFOLD Signals
SCAFFOLD The Biomaterial that is used for tissueengineering applications often serve as scaffold for a specific cell type Natural or synthetic Provide framework, mechanical strength Promotes natural healing Supports cell adhesion and proliferation Carry living cells, drugs, and growth factors Biocompatible, biodegradable
Non invasive manner Hydrogels Injectable delivery method Easy to apply No scar formation Osseoconductive Can adapt to irregular defects such as bony cranial defects Examples Alginate Collagen Gelatin Fibrin Agarose Polyvinyl alcohol
Self Assembling Injectable hydrogel Scaffolds Cells Self assembling peptide hydrogel Cell gel Mix Injection In Situ Gelation
INJECTABLE HYDROGEL: PURAMATIXTM
CELL- SCAFFOLD SYSTEM
Culture of Human Gingiva Derived Mesenchymal Stem Cells HGMSCs Plated in T75 flask DAY 0 HGMSCs DAY 1 HGMSCs at sub-confluence HGMSCs at confluence
Flow-cytometry
ALP Enzyme activity HGMSCS Osteogenic Differentiation GENE Expression 200 1 week 2 weeks 180 160 140 * * ALP Type I Collagen 120 100 80 Control OM CM OM CM OM B actin Endogenous control 60 40 20 0 1 week 2 weeks
Protein Expression 1 Week 2 Weeks OPN Beta Actin Osteopontin Osteopontin
MINERAL DEPOSITION A. ALIZARIN RED Cells cultured in basal medium Cells treated with osteogenic medium B. VON KOSSA STAINING Cells cultured in basal medium Cells treated with osteogenic medium
Cells Encapsulated in Puramatrix TM Cells encapsulated in PuraMatrix hydrogel; Phase contrast images showing the morphology and cell proliferation at different time points. A) Day 1- Cells show round structures. B) Day 3- Cells attained spindle shape- cell growth can be observed.
Cells Encapsulated in Puramatrix TM A) Cells encapsulated in PuraMatrix in terconections B) Day 5- Cells at peripheral region
Absorbance Values Cell Proliferation in 3 D Gel 10,000 30,000 300,000 4.50 4.00 * 3.50 3.00 2.50 2.00 1.50 1.00 0.50 0.00 DAY1 DAY2 DAY3
LIVE DEAD CELL ASSAY Live/Dead Cell Assay at day 1, 3, 5, and 7. Fluorescent microscope pictures - cells in PuraMatrix TM hydrogel with Live/Dead staining. A) Day 1-Cells encapsulated in puramatrix B) Day 3- Cells with spindle shape and they are spread out evenly. C) Day 5 Cells are alive and express growth. D) Day-7 Cells have increased in proliferation and show adhesion to fibrous network.
SCANNING ELECTRON MICROSCOPY STUDIES SEM of PuraMatrix TM and HGMSCs seeded PuraMatrix TM. A) Scanning electron microscopy of PuraMatrix TM scaffold only. A.1 Shows surface appearing like a sheet under low magnification, 187x. A.2 Shows peptides appearance to be like interwoven nanofibers at higher magnification, 483x. B) Scanning electron microscopy of PuraMatrix TM with HGMSC cells. B.1 PuraMatrix TM with HGMSC under 577x magnification. Shows linear assembly of cells within matrix. B.2 PuraMatrix TM with HGMSC under 629x magnification. Shows linear assembly of cells within matrix
OSTEOGENIC DIFFERENTIATION Gene expression Studies
Mineralization HGMSCs as monolayer culture (2D) and cells encapsulated in PuraMatrix (3-D). The morphology of differentiated cells A) Cells in monolayer in osteogenic medium at week 4 B) Cells induced with OM for 4 weeks and stained with Alizarin Red orange color indicates calcium deposition C) Cells in PuraMatrix in OM (clustering of cells can be observed) F) 4 weeks -Cells in PuraMatrix were stained with Alizarin Red to detect the mineral deposit, presence of mineral deposition is observed for cells with in PuraMatrix gel.
Summary of In Vitro Study HGMSCs demonstrated osteogenic differentiation The cells grown in PuraMatrix nanoscaffold showed high survival rate and cell growth was also observed in time dependent manner The cells attained spindle shape within 3 days of encapsulation and cell growth was observed from day 3 Scanning electron microscope studies revealed that the cell bodies embedded in PuraMatrix started to develop a dense network process. The Live/Dead cell assay and WST assay revealed that PuraMatrix nanofibers are cytocompatible Cells expressed positive mineralization at 4 weeks
INJECTION OF CELLS AND SCAFFOLD
CT SCAN CT Scans of Control and Week 2. Series of images from CT Scan of rat subject post surgery using i- CAT vision software showing 2D scans, 3D scans, and control and experiment cross sectional slices. A) CT scans of control rat shows no radiopacity at week 4. B) Shows 2 week CT scan of rats showing radiopacities starting to form.
CT SCAN A) Clusters of radiopacities presented on injectable experimental side at 4 weeks. B) 3D representation of radiopacities at 4 weeks. C) Clusters of radiopacities presented on injectable experimental side at 4 weeks. D) 3D representation of radiopacities at 4 weeks.
Ct Scan Clusters of radiopacities presented on injectable experimental side at 4 weeks.
Histology Histological slides at 400x. A) Bone tissue formation at 4 weeks. B) Bone tissue formation at 4 weeks. C) Bone tissue at 4 weeks. D) 2mm bone nodule explant excised from dorsum of rat at 4 weeks.
Histology A) Tissue sample of control side showing connective tissue only. B) Tissue sample of control side showing presence of remanants of PuraMatrix scaffold.
ANIMAL MODEL
Summary: In vivo Study In Vivo Study CT scans show radiopacities suggesting that PuraMatrix scaffold with HGMSC supported ectopic bone formation Histological studies demonstrated that PuraMatrix in combination HGMSCs supported the ectopic bone formation. We are establishing the animal model
CONCLUSIONS AND FUTURE STUDY The self-assembled, injectable PuraMatrix scaffold in combination with HGMSCs can support bone tissue formation Further research needed to investigate the bone growth in terms of density and volume at week 8 and later time points. Also, further studies will investigate the potential of HGMSCs seeded PuraMatrix combination for the repair of critical size defects in hard palate of rats. Using growth factors to enhance bone growth
CELL CULTURE AND BEAD GENERATION 2% alginate (w/v) solution Beads ~30mg,60mg,120mg Ca++
Cell Encapsulation ENCAPSULATED CELLS
Acknowledgements Don Do MD Reem Almashat DDS Nora Al Amer DDS Casey Lynn Debbie Stiles Ross Brockman Jason Portnof MD